Structure and developmental expression of Ikaros in the Mexican axolotl

Citation
C. Durand et al., Structure and developmental expression of Ikaros in the Mexican axolotl, IMMUNOGENET, 50(5-6), 1999, pp. 336-343
Citations number
39
Categorie Soggetti
Immunology
Journal title
IMMUNOGENETICS
ISSN journal
00937711 → ACNP
Volume
50
Issue
5-6
Year of publication
1999
Pages
336 - 343
Database
ISI
SICI code
0093-7711(199912)50:5-6<336:SADEOI>2.0.ZU;2-8
Abstract
The Ikaros family of transcription factors plays an essential role in hemat opoiesis. We report here the structure of cDNA clones encoding two Ikaros i soforms, Ik1 and Ik2, in the Mexican axolotl. The Ik1 cDNA sequence is very similar to that of the rainbow trout, chicken, and mammalian Ik1 sequences . However, a 96 base pair region which encodes the first N-terminal zing fi nger (F1) is lacking from axolotl Ik1, both in clones from a cDNA library a nd clones isolated from direct polymerase chain reaction products. A region corresponding to exon 3 is completely absent from the axolotl Ik2 sequence and thus the Ik1 and Ik2 isoforms possess the same number of zinc finger m otifs. The structure of these five CC-HH motifs is very well conserved in t he axolotl, including the structural deviations from its amino acid consens us composition which are identical in all species analyzed to date. The axo lot1 Ik1 3' untranslated region sequence is very long (2538 bp) and contain s two UA-rich motifs known as instability determinants and which could play a role in mRNA translational efficiency. Ikaros transcripts are first dete cted in the ventral blood island of stage 36 embryos, about 24h before the first heartbeats (late tailbud stage), and then in the major lymphopoietic organs of the developing larvae. In situ hybridization demonstrates that Ik aros transcripts are abundant at the periphery of the thymus lobes, in the presumptive site of early thymocyte differentiation.